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Cervical Recuperation After Vaginal Delivery

R

Rambam Health Care Campus

Status

Completed

Conditions

Cervix

Treatments

Device: Trans-vaginal ultrasound

Study type

Observational

Funder types

Other

Identifiers

NCT03034434
0154-16-RMB

Details and patient eligibility

About

Patients after vaginal delivery will undergo 3 trans-vaginal ultrasounds in order to examine the process of cervical recuperation post delivery.

Full description

Patients after vaginal delivery will be recruited after receiving a full explanation and signing an informed consent.

The goal of the study is to examine cervical length after vaginal delivery at 3 different time intervals:

  1. 8 hours post delivery.
  2. 24 hours post delivery.
  3. 48 hours post delivery. At each interval a trans-vaginal ultrasound will be performed, evaluating cervical length. At the end of the 3rd and final ultrasound, the patient will finish her participation in the study/ Information regarding obstetric conditions such as labor induction, gestational age at the time of delivery etc. will be collected from patients' electronic files.

Enrollment

1,384 patients

Sex

Female

Ages

18 to 44 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Any patient after vaginal delivery.

Exclusion criteria

  • Any patient after cesarean section.

Trial design

1,384 participants in 1 patient group

Patients after vaginal delivery
Description:
Patients after vaginal delivery willing to undergo 3 trans-vaginal ultrasounds within the 48 hours after delivery.
Treatment:
Device: Trans-vaginal ultrasound

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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